Canonical Allele Identifier: CA359563333

Gene: RICTOR

Linked Data

• MyVariant Identifiers: chr5:g.38955701G>A (hg19) ; chr5:g.38955599G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38955599G>A , CM000667.2:g.38955599G>A	GRCh38
NC_000005.9:g.38955701G>A , CM000667.1:g.38955701G>A	GRCh37
NC_000005.8:g.38991458G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296782.10:c.2605C>T	ENSP00000296782.5:p.Gln869Ter
ENST00000503698.2:c.565C>T	ENSP00000518563.1:p.Gln189Ter
ENST00000514735.2:c.2557C>T	ENSP00000423162.2:p.Gln853Ter
ENST00000711063.1:c.2605C>T	ENSP00000518562.1:p.Gln869Ter
ENST00000357387.8:c.2605C>T MANE Select	ENSP00000349959.3:p.Gln869Ter
ENST00000296782.9:c.2605C>T	ENSP00000296782.5:p.Gln869Ter
ENST00000357387.7:c.2605C>T	ENSP00000349959.3:p.Gln869Ter
ENST00000503698.1:n.565C>T
ENST00000511516.5:c.*1829C>T	ENSP00000423019.1:n.*1829C>T
NM_001285439.1:c.2605C>T	NP_001272368.1:p.Gln869Ter
NM_001285440.1:c.1750C>T	NP_001272369.1:p.Gln584Ter
NM_152756.4:c.2605C>T	NP_689969.2:p.Gln869Ter
XM_006714463.2:c.2605C>T	XP_006714526.1:p.Gln869Ter
XM_011514005.1:c.2605C>T	XP_011512307.1:p.Gln869Ter
XM_011514006.1:c.2416C>T	XP_011512308.1:p.Gln806Ter
XM_011514007.1:c.1750C>T	XP_011512309.1:p.Gln584Ter
XM_006714463.3:c.2605C>T	XP_006714526.1:p.Gln869Ter
XM_011514005.2:c.2605C>T	XP_011512307.1:p.Gln869Ter
XM_011514006.3:c.2416C>T	XP_011512308.1:p.Gln806Ter
XM_017009311.1:c.2557C>T	XP_016864800.1:p.Gln853Ter
XM_017009312.1:c.2557C>T	XP_016864801.1:p.Gln853Ter
XM_017009313.1:c.2446C>T	XP_016864802.1:p.Gln816Ter
XM_017009314.2:c.1750C>T	XP_016864803.1:p.Gln584Ter
XM_017009315.2:c.1750C>T	XP_016864804.1:p.Gln584Ter
NM_152756.5:c.2605C>T MANE Select	NP_689969.2:p.Gln869Ter
NM_001285439.2:c.2605C>T	NP_001272368.1:p.Gln869Ter
NM_001285440.2:c.1750C>T	NP_001272369.1:p.Gln584Ter